Investigation of the effect of acylation on the enantiomeric separation of amino acid isopropyl esters by gas chromatography
β Scribed by Xianwen Lou; Xueliang Liu; Daoqian Zhu; Qinghai Wang; Liangmo Zhou
- Book ID
- 107781724
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 546 KB
- Volume
- 626
- Category
- Article
- ISSN
- 1873-3778
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## Abstract Racemic amino alcohols have been separated as perfluoroacylated derivatives by gas chromatography using either improved ChirasilβVal or heptakis(2,6βdiβ__O__βmethylβ3β__O__βpentyl)βΞ²βcyclodextrin as stationary phase. Using ChirasilβVal all the amino alcohols investigated were separated
A previously described procedure for determining the enantiomeric ratios of amino acids has produced inconsistent results when determining relatively low (~0.110) D/L ratios. The method involves synthesis of diastereomeric N-trifluoroacetyl-L-prolyl-D/L-amino acid ester dipeptides which are resolved